Team:Frankfurt/Notebook
From 2012.igem.org
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You should make use of the calendar feature on the wiki and start a lab notebook. This may be looked at by the judges to see how your work progressed throughout the summer. It is a very useful organizational tool as well. | You should make use of the calendar feature on the wiki and start a lab notebook. This may be looked at by the judges to see how your work progressed throughout the summer. It is a very useful organizational tool as well. | ||
- | + | =Methods and Protocols= | |
- | =Culture Medium= | + | ==Culture Medium== |
{|class=wikitable float:right | {|class=wikitable float:right | ||
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pH has to be regulated with NaOH to pH=7.5 | pH has to be regulated with NaOH to pH=7.5 | ||
- | <br> | + | <br> <br> |
Every cluture medium has to be autoclaved. | Every cluture medium has to be autoclaved. | ||
- | + | =Agar Plate= | |
+ | ===LB<sup>ampicillin</sub>-Agar=== | ||
+ | Add 2 % agar to LB-medium. After autoclaving and cooling-down to 60 °C steril ampicillin is added. Plates were poured. | ||
+ | ===SCD-Agar=== | ||
+ | Add 2 % agar to SCD-medium. After autoclaving and cooling-down steril amino acid solution is added. Dependent on the respective selective medium Histidin (0.25 mM), Trypthophan (0.19 mM), Uracil (0.44 mM) or Leucin (0.35 mM) is added. | ||
+ | ===YEPD-Agar=== | ||
+ | Add 2 % agar to YEPD-medium |
Revision as of 14:32, 14 September 2012
Home | Team | Project | Organisms | New Yeast RFC | Notebook | Registered Parts | Modeling | Safety | Attributions | Official Team Profile |
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You should make use of the calendar feature on the wiki and start a lab notebook. This may be looked at by the judges to see how your work progressed throughout the summer. It is a very useful organizational tool as well.
Contents |
Methods and Protocols
Culture Medium
Full Medium (YEPD) for Yeast | |||
---|---|---|---|
Yeast Extract | 1 % (weight/volume) | ||
Pepton | 2 % (w/v) | ||
Glucose | 2 % (w/v) |
Synthetic Complete Medium (SC) for Yeast | |||
---|---|---|---|
Yeast Nitrogen Base | 0.17 % (w/v) | ||
Ammoniumsulfate | 0.5 % (w/v) | ||
Amino Acid Mix* | 50 ml/l | ||
Histidin** | 0.25 mM | ||
Tryptophan** | 0.19 mM | ||
Leucin** | 0.35 mM | ||
Uracil** | 0.44 mM |
pH has to be regulated with KOH to pH=6.3
!* contains no His, Leu, Trp and Uracil
** addition of this components depents on the respective selection medium
SOC-Medium for Regeneration of transformed Escherichia coli`s after Electroporation | |||
---|---|---|---|
Trypton | 2 % (w/v) | ||
Yeast Extract | 0.5 % (w/v) | ||
NaCl | 10 mM | ||
KCl | 2,5 mM | ||
MgCl2 | 10 mM | ||
MgSO4 | 10 mM | ||
Glucose | 20 mM |
pH has to be regulated to pH=6.8-7.0
Full Medium (YEPD) for Yeast | |||
---|---|---|---|
Yeast Extract | 1 % (weight/volume) | ||
Trypton | 0.5 % (w/v) | ||
NaCl | 0.5 % (w/v) |
pH has to be regulated with NaOH to pH=7.5
Every cluture medium has to be autoclaved.
Agar Plate
LBampicillin</sub>-Agar
Add 2 % agar to LB-medium. After autoclaving and cooling-down to 60 °C steril ampicillin is added. Plates were poured.
SCD-Agar
Add 2 % agar to SCD-medium. After autoclaving and cooling-down steril amino acid solution is added. Dependent on the respective selective medium Histidin (0.25 mM), Trypthophan (0.19 mM), Uracil (0.44 mM) or Leucin (0.35 mM) is added.
YEPD-Agar
Add 2 % agar to YEPD-medium